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A novel GlnR target gene, nnaR, is involved in nitrate/nitrite assimilation in Streptomyces coelicolor

机译:NNAR的新型GLNR靶基因,涉及链霉菌的硝酸盐/亚硝酸盐同化

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GlnR is the global transcriptional regulator of nitrogen assimilation in Streptomyces coelicolor. Under nitrogen starvation, GlnR controls the transcription of at least nine genes associated with nitrogen metabolism. In this study, we identified a new GlnR target gene, SCO2958, named nnaR (nitrate/nitrite assimilation regulator). In silico analysis of NnaR revealed the presence of two distinct domains: an N-terminal uroporphyrinogen-III synthase (HemD)-like enzymatic domain and a C-terminal DNA binding domain. Complementation experiments with a haemin auxotroph Escherichia coli ΔhemD mutant strain revealed that NnaR has no HemD activity. Physiological studies of an S. coelicolor nnaR?:?:?Tn5062 mutant showed that NnaR is involved in regulating nitrite reduction. By electrophoretic mobility shift assays the functionality of the NnaR DNA binding domain was confirmed, and it was found that NnaR binds in front of the genes narK (putative nitrate extrusion protein), nirB (nitrite reductase), nirA (putative nitrite/sulphite reductase) and nasA (putative nitrate reductase), which are associated with nitrate/nitrite assimilation. Furthermore, a cooperative binding of NnaR together with GlnR to the nirB promoter was observed, suggesting that NnaR may act as a GlnR co-activator.
机译:GLNR是Streptomyces Coelicolor中氮素同化的全局转录调节因子。在氮饥饿下,GLNR控制与氮代谢相关的至少九个基因的转录。在这项研究中,我们确定了一种新的GLNR靶基因,SCO2958,名为NNAR(硝酸盐/亚硝酸盐同化调节剂)。在NNAR的硅分析中,揭示了两个不同的结构域的存在:N-末端尿卟啉-III合酶(HEMD) - 样酶结构域和C末端DNA结合结构域。具有血红素滋巢疗法大肠杆菌ΔHemd突变菌株的互补实验显示,NNAR没有HEMD活性。 S. coelicolor nnar的生理学研究?:?:TN5062突变体显示NNAR参与调节亚硝​​酸盐还原。通过电泳迁移率移位测定NNAR DNA结合结构域的功能得到证实,发现NNAR在基因芽(推注硝酸盐挤出蛋白),NIRB(亚硝酸盐还原酶),NIRA(推定亚硝酸盐/亚硫酸盐还原酶)中结合和NASA(推注硝酸还原酶),与硝酸盐/亚硝酸盐同化相关。此外,观察到NNAR与GLNR一起与NIRB启动子的合作结合,表明NNAR可以充当GLNR共激活剂。

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